Product Description
Disintegration Test App, I.P. Standard (Double Basket):- The test equipment work on up and down movement of tablet in medium of water kept at 37^C. A geared motor for the vertical shaft drive the shaft moves up and down by 7.5 cms at speed of 30 per minute. On the upper end of the shaft fitted horizontal strip with clamp on either side. These clamps hold glass vessels open at the both ends and with stainless steel wire gauge with rubber rings at the lower end, which dips in water. Two independently thermostatically controlled hot plate rating 65 watt are fixed on the top of the cabinet upon which beakers of 1000 ml size are net filled with water. Temperature is mainted at 37^ C with and accuracy of 1^ C. Independent switches with neon indicators for motor hot plates are fitted on a panel. Mains fuse with two meters cord and plug provided work on 220 volts A.C. mains.
Reliable Disintegration TestingEnsure accurate and repeatable disintegration testing of tablets and capsules using this robust test apparatus, engineered from mild steel and quality components. Designed to meet pharmaceutical regulatory standards, it offers precise temperature control and a versatile voltage range, making it suitable for diverse laboratory environments. The inclusion of borosilicate water baths promotes thermal stability, while the programmable digital timer supports ease of operation and consistency.
Standard-Compliant and User-FriendlyThis apparatus is built for laboratories seeking compliance with major pharmacopoeias such as USP, IP, and BP. Routine operations are simplified with features like standard 1000 ml beakers, manual basket lift with locking, and a digital programmable timer for accurate monitoring. Maintenance requirements are minimal due to the robust construction and water-resistant materials.
FAQs of Disintegration Test Apparatus:
Q: How does the Disintegration Test Apparatus ensure regulatory compliance?
A: The apparatus is designed to meet the requirements of international standards such as USP, IP, and BP, ensuring its suitability for official lab use and inspection purposes.
Q: What is the process for conducting a test on this apparatus?
A: To perform a test, place tablets or capsules in the supplied baskets, immerse them in 1000 ml beakers filled with water, set the temperature and timer using the digital interface, and observe the disintegration as per regulatory protocols.
Q: When should I use this apparatus in pharmaceutical testing?
A: This equipment is essential during formulation development, routine quality control, and batch release procedures to verify that oral dosage forms break down properly within specified time limits.
Q: Where is the apparatus best utilized?
A: It is ideally used in pharmaceutical laboratories, research and development centers, universities, and industrial quality assurance labs that require reliable disintegration analysis.
Q: What are the main benefits of using this disintegration tester?
A: Key benefits include consistent results, regulatory compliance, efficient temperature control with borosilicate water baths, ease of use with a programmable timer, and robust mild steel construction for durability.
Q: How do I maintain the apparatus for long-term use?
A: Maintenance involves regular cleaning of the beakers and water bath, ensuring the heater is kept free of scale, and periodic inspection of the manual lift mechanism and timer to ensure reliable operation.